Results for 'Patented drugs'

473 found
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  1.  46
    Patents on drugs – the wrong prescription?Peter Dietsch - 2008 - In Axel Gosseries, Alain Marciano & Alain Strowel, Intellectual Property and Theories of Justice. Basingstoke & N.Y.: Palgrave McMillan. pp. 230-245.
    Theories of justice and intellectual property are vast topics in their own right. The contributions to this volume examine how they relate. How do our justifications for protecting intellectual property fare from an ethical perspective? Any attempt to tackle this question in a relatively short chapter like this one will have to be restricted in scope. My claims are limited in four ways. First, I concentrate on one kind of intellectual property protection, namely patents. Second, the claims of justice put (...)
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  2. Exploring Regulatory Flexibility to Create Novel Incentives to Optimize Drug Discovery.Jacqueline A. Sullivan & E. Richard Gold - 2024 - Frontiers in Medicine 11 (Section on Regulatory Science).
    Efforts by governments, firms, and patients to deliver pioneering drugs for critical health needs face a challenge of diminishing efficiency in developing those medicines. While multi-sectoral collaborations involving firms, researchers, patients, and policymakers are widely recognized as crucial for countering this decline, existing incentives to engage in drug development predominantly target drug manufacturers and thereby do little to stimulate collaborative innovation. In this mini review, we consider the unexplored potential within pharmaceutical regulations to create novel incentives to encourage a (...)
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  3. Time discounting, consistency, and special obligations: a defence of Robust Temporalism.Harry R. Lloyd - 2021 - Global Priorities Institute, Working Papers 2021 (11):1-38.
    This paper defends the claim that mere temporal proximity always and without exception strengthens certain moral duties, including the duty to save – call this view Robust Temporalism. Although almost all other moral philosophers dismiss Robust Temporalism out of hand, I argue that it is prima facie intuitively plausible, and that it is analogous to a view about special obligations that many philosophers already accept. I also defend Robust Temporalism against several common objections, and I highlight its relevance to a (...)
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  4. The Impact of Nanomedicine Development on North–South Equity and Equal Opportunities in Healthcare.Michael G. Tyshenko - 2009 - Studies in Ethics, Law, and Technology 3 (3).
    Nanomedicine applications are an extension of traditional pharmaceutical drug development that are targeting the most pressing health concerns through improvements to diagnostics, drug delivery systems, therapeutics, equipment, surgery and prosthetics. The benefits and risks to the individual have been extrapolated to include broader societal impacts of nanomedicine with concerns extending to inequitable distribution of benefits accruing to developed, or North countries, rather than developing, or South countries. Analysis reveals a great deal of overlap between the North and South's most serious (...)
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  5. Patently paradoxical? 'Public order' and genetic patents.Donna Dickenson - 2004 - Nature Reviews Genetics 5 (2):86.
    How heavily should ethical considerations weigh in allowing or disallowing genetic patents? The concept of 'ordre public' can be useful in offsetting a simple utilitarian view.
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  6. On Drugs.Sam Baron, Sara Linton & Maureen A. O’Malley - 2023 - Journal of Medicine and Philosophy 48 (6):551-564.
    Despite their centrality to medicine, drugs are not easily defined. We introduce two desiderata for a basic definition of medical drugs. It should: (a) capture everything considered to be a drug in medical contexts and (b) rule out anything that is not considered to be a drug. After canvassing a range of options, we find that no single definition of drugs can satisfy both desiderata. We conclude with three responses to our exploration of the drug concept: maintain (...)
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  7. Drug Familiarization and Therapeutic Misconception Via Direct-to-Consumer Information.Jean-Christophe Bélisle-Pipon & Bryn Williams-Jones - 2015 - Journal of Bioethical Inquiry 12 (2):259-267.
    Promotion of prescription drugs may appear to be severely limited in some jurisdictions due to restrictions on direct-to-consumer advertising. However, in most jurisdictions, strategies exist to raise consumer awareness about prescription drugs, notably through the deployment of direct-to-consumer information campaigns that encourage patients to seek help for particular medical conditions. In Canada, DTCI is presented by industry and regulated by Health Canada as being purely informational activities, but their design and integration in broader promotional campaigns raise very similar (...)
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  8. Drug Regulation and the Inductive Risk Calculus.Jacob Stegenga - 2017 - In Kevin Christopher Elliott & Ted Richards, Exploring Inductive Risk: Case Studies of Values in Science. New York: Oup Usa. pp. 17-36.
    Drug regulation is fraught with inductive risk. Regulators must make a prediction about whether or not an experimental pharmaceutical will be effective and relatively safe when used by typical patients, and such predictions are based on a complex, indeterminate, and incomplete evidential basis. Such inductive risk has important practical consequences. If regulators reject an experimental drug when it in fact has a favourable benefit/harm profile, then a valuable intervention is denied to the public and a company’s material interests are needlessly (...)
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  9. Disagreement, Drugs, etc.: from Accuracy to Akrasia.David Christensen - 2016 - Episteme 13 (4):397-422.
    We often get evidence concerning the reliability of our own thinking about some particular matter. This “higher-order evidence” can come from the disagreement of others, or from information about our being subject to the effects of drugs, fatigue, emotional ties, implicit biases, etc. This paper examines some pros and cons of two fairly general models for accommodating higher-order evidence. The one that currently seems most promising also turns out to have the consequence that epistemic akrasia should occur more frequently (...)
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  10. Drug-Induced Body Disownership.Raphaël Millière - 2024 - In Chris Letheby & Philip Gerrans, Philosophical Perspectives on Psychedelic Psychiatry. Oxford University Press.
    In recent years, a debate has emerged on whether bodily sensations are typically accompanied by a sense of body ownership, namely a distinctive experience of one's body or body part as one's own. Realists about the sense of body ownership heavily rely on evidence from experimentally-induced bodily illusions (e.g., the rubber hand illusion) and pathological disownership syndromes (e.g. somatoparaphrenia). In this chapter, I will introduce novel evidence regarding body disownership syndromes induced by psychoactive drugs rather than pathological conditions, and (...)
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  11. Drug Laws, Ethics, and History.Adam Greif - 2019 - Filozofia 74 (2):95 - 110.
    In this paper, I present and criticize several historical arguments in favour of prohibition and criminalization of illicit psychoactive substances. I consider several versions of Charles Brent’s argument from drug harms and an argument from addiction based on Kantian view on autonomy. My criticism will mainly rely on empirical evidence on drugs, drug use, and addiction. I think that in light of this evidence, all of the arguments lose their cogency or can be refuted altogether. Moreover, the evidence reveals (...)
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  12. Taking Drugs to Help Others.Thomas Douglas - 2016 - In David Edmonds, Philosophers Take on the World. Oxford University Press UK.
    Every day the news shows us provoking stories about what's going on in the world, about events which raise moral questions and problems. In Philosophers Take On the World a team of philosophers get to grips with a variety of these controversial issues, from the amusing to the shocking, in short, engaging, often controversial pieces. This chapter covers drug use, making you think again about the judgements we make on a daily basis and the ways in which we choose to (...)
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  13.  36
    Evolving Drug Discovery: Artificial Intelligence and Machine Learning's Impact in Pharmaceutical Research.Palakurti Naga Ramesh - 2023 - Esp Journal of Engineering and Technology Advancements 3 (1):136-147.
    The integration of Artificial Intelligence (AI) and Machine Learning (ML) into the research landscape has transforming almost every extending field, including pharmaceutical research. The idea of drug discovery itself is very conventional and has long been criticized for being overly lengthy and expensive, which sometimes may take more than 10 years and billions of dollars to develop a certain drug. AI and ML formulate the future of the drug discovery process by using big data to provide preliminary drug candidates more (...)
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  14. Patentes farmacéuticas.Iván Vargas-Chaves - 2017 - Salamanca: Editorial Ratio Legis.
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  15. Is It Ethical To Patent Human Genes?Annabelle Lever - 2008 - In Axel Gosseries, Alain Marciano & Alain Strowel, Intellectual Property and Theories of Justice. Basingstoke & N.Y.: Palgrave McMillan. pp. 246--64.
    This paper examines the claims that moral objections to the patenting of human genes are misplaced and rest on confusions about what a patent is, or what is patented by a human gene patent. It shows that theese objections rest on too simple a conception of property rights, and the connections betwteen familiar moral objections to private property and moral objections to the patenting of human genes. Above all, the paper claims, objections to HGPs often reflect worries about the (...)
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  16. Revolutionizing Drug Discovery: The Role of Artificial Intelligence in Accelerating Pharmaceutical Innovation".Alaa Soliman Abu Mettleq, Alaa N. Akkila, Mohammed A. Alkahlout, Suheir H. A. ALmurshidi, Bassem S. Abu-Nasser & Samy S. Abu-Naser - 2024 - Information Journal of Academic Engineering Research (Ijaer) 8 (10):45-53.
    Abstract: The integration of artificial intelligence (AI) into drug discovery is revolutionizing the pharmaceutical industry by accelerating the development of novel therapeutics. AI-powered tools enable researchers to process vast datasets, identify drug candidates, and predict their efficacy and safety with unprecedented speed and accuracy. This paper explores the transformative impact of AI on drug discovery, highlighting key advancements in machine learning algorithms, deep learning, and predictive modeling. Additionally, it addresses the challenges associated with AI implementation, including data quality, regulatory hurdles, (...)
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  17. DRUG FACTS, VALUES, AND THE MORNING-AFTER PILL.Christopher ChoGlueck - 2021 - Public Affairs Quarterly 35 (1):51-82.
    While the Value-Free Ideal of science has suffered compelling criticism, some advocates like Gregor Betz continue to argue that science policy advisors should avoid value judgments by hedging their hypotheses. This approach depends on a mistaken understanding of the relations between facts and values in regulatory science. My case study involves the morning-after pill Plan B and the “Drug Fact” that it “may” prevent implantation. I analyze the operative values, which I call zygote-centrism, responsible for this hedged drug label. Then, (...)
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  18. Why are Software Patents so Elusive? A Platonic Approach.Odin Kroeger - 2011 - Masaryk University Journal of Law and Technology 5 (1):57-70.
    Software patents are commonly criticised for being fuzzy, context-sensitive, and often granted for trivial inventions. More often than not, these shortcomings are said to be caused by the abstract nature of software - with little further analysis offered. Drawing on Plato’s Parmenides, this paper will argue (1) that the reason why software patents seem to be elusive is that patent law suggests to think about algorithms as paradigmatic examples and (2) that Plato’s distinction between two modes of predication and the (...)
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  19. The aesthetics of drugs.C. Thi Nguyen - 2024 - In Rob Lovering, The Palgrave Handbook of Philosophy and Psychoactive Drug Use. New York: Palgrave Macmillan.
    The aesthetics of tea, in some practices, seems to focus on appreciating the mental effects of tea — the altered states of mind. Wine aesthetics, on the other hand, seems to actively exclude any inebriative effects. Wine experts are supposed to spit, in order to avoid inebriation when they judge wine. Why? The answer, I suggest, lies deep in several key suppositions in the traditional model of aesthetic experience: that aesthetic experience needs to be accurate of its object, and that (...)
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  20. Are pharmaceutical patents protected by human rights?Joseph Millum - 2008 - Journal of Medical Ethics 34 (11):e25-e25.
    The International Bill of Rights enshrines a right to health, which includes a right to access essential medicines. This right frequently appears to conflict with the intellectual property regime that governs pharmaceutical patents. However, there is also a human right that protects creative works, including scientific productions. Does this right support intellectual property protections, even when they may negatively affect health? -/- This article examines the recent attempt by the Committee on Economic, Social and Cultural Rights to resolve this issue (...)
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  21. ILLICIT DRUG USE AND TRADE: AN ETHNOGRAPHIC STUDY OF KUMASE (2000–2018).Samuel Adu-Gyamfi, Ali Yakubu Nyaaba, Kwasi Amakye-Boateng, Daniel Owusu-Ansah & Michael Nimoh - 2020 - Sociological Studies 26 (1):59-81.
    The illegal drug trade is a world phenomenon, which has had some adverse impact on societies. Significantly, the impact is damning in developing economies in Africa and Ghana in particular. This paper therefore seeks to address the causes and effects of the use and peddle of these illegal drugs in three communities in the capital city of the Asante Region of Ghana. It further ascertains the extent to which these drugs burden the security agencies in the communities and (...)
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  22. Multi drug therapy effects on routine laboratory parameters in Leprosy patients.Tanjimul Islam & Rubab Tarannum Islam - 2016 - International Journal of Sciences and Applied Research 3 (3):13-19.
    Background: Multi Drug Therapy approved by WHO is the best treatment option for Leprosy. There is a significant decline of mortality and morbidity after the introduction of multi drug therapy. But the adverse effects causing changes in clinical and laboratory parameters to multi drug therapy are the main limiting obstacle for the treatment course completion. Objective: The aim of this study is to find out the effects on routine laboratory parameters including hematological and biochemical changes before, during and after the (...)
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  23. Psilocybin, LSD, Mescaline and drug-induced synesthesia.Dimitria Electra Gatzia & Berit Brogaard - 2016 - In Victor R. Preedy, The Neuropathology Of Drug Addictions And Substance Misuse. Elsevier.
    Studies have shown that both serotonin and glutamate receptor systems play a crucial role in the mechanisms underlying drug-induced synesthesia. The specific nature of these mechanisms, however, continues to remain elusive. Here we propose two distinct hypotheses for how synesthesia triggered by hallucinogens in the serotonin-agonist family may occur. One hypothesis is that the drug-induced destabilization of thalamic projections via GABAergic neuronal circuits from sensory areas leads to a disruption of low-level, spontaneous integration of multisensory stimuli. This sort of integration (...)
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  24. The Moral Culture of Drug Prohibition.Ed D’Angelo - 1994 - The Humanist 54 (5):1-7.
    The War on Drugs has been waged primarily for cultural reasons, i.e., to enforce the Protestant Work Ethic. It does not serve a rational utilitarian function.
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  25. Patterns of drug-prescribed and drug-related problems among hospitalized elderly patients.Fathi M. Sherif - 2022 - Mediterreanan Journal of Pharmacy and Pharmaceutical Sciences 2 (2):64-76.
    Prescribing drugs for elderly patients is not an easy task since elderly patients frequently have comorbid conditions. In Libya, there are no guidelines for the management of medications used in elderly patients and no specialized geriatric health institutions. This study aims to assess the pattern of medication use among hospitalized elderly patients in Sebha Medical Centre and the drug-related problems associated with these patterns. This report is a descriptive and retrospective cross-sectional study conducted at Sebha Medical Center in 2021. (...)
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  26. Understanding the pharmaceutical patent system in Spain and Europe: a perspective from the need to take its protection-access tradeoff seriously.Iván Vargas-Chaves & José López-Oliva - 2020 - In Iván Vargas-Chaves & Daniel Alzate-Mora, Derecho y Salud: debates contemporáneos. Sincelejo: Editorial CECAR. pp. 73-86.
    As a result of the doctoral research developed by the main author (Vargas-Chaves, 2017), it was identified the evolution and perspectives of the pharmaceutical patent in the international trade system, as well as it future legal research needs in this topic, both immediate and long-term. Furthermore, a number of problems of public health were highlighted in which the patent-term-extension mechanisms have produced a lack of access to medicines.
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  27. An Argument Against Drug Testing Welfare Recipients.Mary Jean Walker & James Franklin - 2018 - Kennedy Institute of Ethics Journal 28 (3):309-340.
    Programs of drug testing welfare recipients are increasingly common in US states and have been considered elsewhere. Though often intensely debated, such programs are complicated to evaluate because their aims are ambiguous – aims like saving money may be in tension with aims like referring people to treatment. We assess such programs using a proportionality approach, which requires that for ethical acceptability a practice must be: reasonably likely to meet its aims, sufficiently important in purpose as to outweigh harms incurred, (...)
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  28. Impartiality at the Patent Office.Acosta Benedicto - forthcoming - Public Integrity.
    Social contract is one of the most common schemes for justifying patents. According to this theory, inventors obtain a commercial exclusivity in exchange for the disclosure of the invention, with the final aim of allowing others to use that knowledge in future innovations. Under the rationale of this social contract theory of patents, if a patent system is not guided by impartiality in its decisions, the relation between disclosure of inventions and future innovation becomes an issue, because non-merit factors in (...)
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  29. Drug-Induced Alterations of Bodily Awareness.Raphaël Millière - 2022 - In Adrian J. T. Alsmith & Andrea Serino, The Routledge Handbook of Bodily Awareness. Routledge.
    Philosophical and empirical research on bodily awareness has mostly focused so far on bodily disorders – such as anorexia nervosa, somatoparaphrenia, or xenomelia (body integrity dysphoria) – and bodily illusions induced in an experimental setting – such as the rubber hand illusion, or the thermal grid illusion. Studying these conditions can be illuminating to investigate a broad range of issues about the nature, function, and etiology of bodily experience. However, a number of psychoactive compounds can also induce a remarkably wide (...)
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  30. Students’ perspectives on drugs and alcohol abuse at a public university in Zambia.Nicholas Mwanza & Ganizani Mwale - 2023 - HTS Theological Studies 79 (3):8.
    Access to students’ perspectives on substance abuse is essential for effective youth intervention projects development. This study aimed to explore students’ perspectives on abuse of drugs and alcohol with probable development of student-led intervention strategies. The study was conducted at public universities in Zambia. Student’s perspectives on drugs and alcohol abuse were documented using a mixed method design that employed purposive and snowball sampling to select 200 respondents to questionnaires and 10 to in-depth interviews. A humanistic theory approach (...)
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  31. Drug Recommendation System in Medical Emergencies using Machine Learning.S. Venkatesh - 2025 - Journal of Science Technology and Research (JSTAR) 6 (1):1-21.
    In critical medical emergencies, timely and accurate drug recommendation is essential for saving lives and reducing complications. This project proposes a Drug Recommendation System utilizing Machine Learning (ML) techniques to assist healthcare professionals in making quick and accurate drug selections based on patient symptoms, medical history, and emergency condition. The system integrates data from diverse medical databases, including symptoms, diseases, patient demographics, and prior medical records, to recommend the most appropriate drugs or treatments in real-time. The ML model is (...)
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  32. Drug Policy, Paternalism and the Limits of Government Intervention.Daniel Hirst - 2020 - International Journal of Political Theory 4 (1):54-73.
    Gerald Dworkin provides an insightful starting point for determining acceptable paternalism through his commitment to protecting our future autonomy and health from lasting damage. Dworkin grounds his argument in an appeal to inherent goods, which this paper argues is best considered as a commitment to human flourishing. However, socialconnectedness is also fundamental to human flourishing and an important consideration when determining the just limits of paternalistic drug controls, a point missing from Dworkin’ essay. For British philosopher Thomas Hill Green, regulation (...)
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  33. The Myth of Cognitive Enhancement Drugs.Hazem Zohny - 2015 - Neuroethics 8 (3):257-269.
    There are a number of premises underlying much of the vigorous debate on pharmacological cognitive enhancement. Among these are claims in the enhancement literature that such drugs exist and are effective among the cognitively normal. These drugs are deemed to enhance cognition specifically, as opposed to other non-cognitive facets of our psychology, such as mood and motivation. The focus on these drugs as cognitive enhancers also suggests that they raise particular ethical questions, or perhaps more pressing ones, (...)
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  34. (2 other versions)Drugs and Hugs: Stimulating Moral Dispositions as a Method of Moral Enhancement.Michał Klincewicz, Lily Eva Frank & Marta Sokólska - 2018 - Royal Institute of Philosophy Supplement 83:329-350.
    Advocates of moral enhancement through pharmacological, genetic, or other direct interventions sometimes explicitly argue, or assume without argument, that traditional moral education and development is insufficient to bring about moral enhancement. Traditional moral education grounded in a Kohlbergian theory of moral development is indeed unsuitable for that task; however, the psychology of moral development and education has come a long way since then. Recent studies support the view that moral cognition is a higher-order process, unified at a functional level, and (...)
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  35. Drugs That Make You Feel Bad’? Remorse-Based Mitigation and Neurointerventions.Jonathan Pugh & Hannah Maslen - 2017 - Criminal Law and Philosophy 11 (3):499-522.
    In many jurisdictions, an offender’s remorse is considered to be a relevant factor to take into account in mitigation at sentencing. The growing philosophical interest in the use of neurointerventions in criminal justice raises an important question about such remorse-based mitigation: to what extent should technologically facilitated remorse be honoured such that it is permitted the same penal significance as standard instances of remorse? To motivate this question, we begin by sketching a tripartite account of remorse that distinguishes cognitive, affective (...)
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  36. The Ethics of Prescription Drug Monitoring Programs.Ryan Ravanpak - 2023 - Voices in Bioethics 9.
    Prescription Drug Monitoring Programs (PDMPs) contain detailed information about which controlled medications physicians prescribe individuals, including where, when, how much, by whom, and more. The programs allow physicians to glimpse into the life of each patient that visits them — sometimes before a single word is exchanged between them. Every state has a PDMP, and almost all states share the data they collect through it. In this paper, I argue that informed consent should be required for recording of prescriptions related (...)
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  37. Sex, drug and Laruelle.Étienne Brouzes Ebest & Etienne Brouzes - 2007 - Philo-Fictions 1.
    Sex, Drug & Laruelle -/- - et nous errions, nourris du vin des cavernes et du biscuit de la route, moi pressé de trouver le lieu et la formule - A. Rimbaud.
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  38. Racial Justice Requires Ending the War on Drugs.Brian D. Earp, Jonathan Lewis, Carl L. Hart & Walter Veit - 2021 - American Journal of Bioethics 21 (4):4-19.
    Historically, laws and policies to criminalize drug use or possession were rooted in explicit racism, and they continue to wreak havoc on certain racialized communities. We are a group of bioethicists, drug experts, legal scholars, criminal justice researchers, sociologists, psychologists, and other allied professionals who have come together in support of a policy proposal that is evidence-based and ethically recommended. We call for the immediate decriminalization of all so-called recreational drugs and, ultimately, for their timely and appropriate legal regulation. (...)
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  39. Binding Specificity and Causal Selection in Drug Design.Oliver M. Lean - 2020 - Philosophy of Science 87 (1):70-90.
    Binding specificity is a centrally important concept in molecular biology, yet it has received little philosophical attention. Here I aim to remedy this by analyzing binding specificity as a causal property. I focus on the concept’s role in drug design, where it is highly prized and hence directly studied. From a causal perspective, understanding why binding specificity is a valuable property of drugs contributes to an understanding of causal selection—of how and why scientists distinguish between causes, not just causes (...)
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  40. On value-laden patents: a call for moral limits.Acosta Benedicto - forthcoming - International Journal of Ethics and Systems.
    Purpose. The main objective of this article is to discuss the suitability of moral and ordre public clauses, and to advance the view that ethical reflection within patent systems is valuable. Methodology. This is a conceptual paper that draws upon the present situation in Europe to illuminate a discussion of the different views about the morality patents, with particular emphasis on criticism of authors who have espoused a narrow interpretation of moral clauses, such as that adopted by the EPO. Findings. (...)
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  41. A Moral Defense of Recreational Drug Use.Rob Lovering - 2015 - Palgrave Macmillan.
    Why does American law allow the recreational use of some drugs, such as alcohol, tobacco, and caffeine, but not others, such as marijuana, cocaine, and heroin? The answer lies not simply in the harm the use of these drugs might cause, but in the perceived morality—or lack thereof—of their recreational use. Despite strong rhetoric from moral critics of recreational drug use, however, it is surprisingly difficult to discern the reasons they have for deeming the recreational use of (some) (...)
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  42. Pathways to Drug Liberalization: Racial Justice, Public Health, and Human Rights.Jonathan Lewis, Brian D. Earp & Carl L. Hart - 2022 - American Journal of Bioethics 22 (9):W10-W12.
    In our recent article, together with more than 60 of our colleagues, we outlined a proposal for drug policy reform consisting of four specific yet interrelated strategies: (1) de jure decriminalization of all psychoactive substances currently deemed illicit for personal use or possession (so-called “recreational” drugs), accompanied by harm reduction policies and initiatives akin to the Portugal model; (2) expunging criminal convictions for nonviolent offenses pertaining to the use or possession of small quantities of such drugs (and releasing (...)
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  43. Risk assessment of genetically modified food and neoliberalism: An argument for democratizing the regulatory review protocol of the Food and Drug Administration.Zahra Meghani - 2014 - Journal of Agricultural and Environmental Ethics 27 (6):967–989.
    The primary responsibility of the US Food and Drug Administration is to protect public health by ensuring the safety of the food supply. To that end, it sometimes conducts risk assessments of novel food products, such as genetically modified food. The FDA describes its regulatory review of GM food as a purely scientific activity, untainted by any normative considerations. This paper provides evidence that the regulatory agency is not justified in making that claim. It is argued that the FDA’s policy (...)
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  44. Cuando el sistema de patentes afecta al bienestar de las personas.Benedicto Acosta & Elisa Calleja-Sordo - forthcoming - Tópicos.
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  45. Responding to Unexpected Urine Drug Test Results: A Phenomenological Approach.Casey Rentmeester - 2023 - Journal of Applied Hermeneutics 2023:1-12.
    As a response to the opioid epidemic in the United States, the Centers for Disease Control and Prevention (CDC) published the CDC Guideline for Prescribing Opioids for Chronic Pain in 2016. This document served as a means to reduce risks and address harms of opioid use by recommending that clinicians conduct periodic urine drug testing for patients on chronic opioid therapy. As an unintended result of this recommendation, providers began using unexpected urine drug test results as a reason to dismiss (...)
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  46. Just Say No (For Now): The Ethics of Illegal Drug Use.Mathieu Doucet - 2017 - Law Ethics and Philosophy 5:9-29.
    The war on drugs is widely criticized as unjust. The idea that the laws prohibiting drugs are unjust can easily lead to the conclusion that those laws do not deserve our respect, so that our only moral reason to obey them flows from a general moral obligation to obey the law, rather than from anything morally troubling about drug use itself. In this paper, I argue that this line of thinking is mistaken. I begin by arguing that the (...)
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  47. Effect of beverages on the disintegration time of drugs in the tablet dosage form.Fathi M. Sherif - 2024 - Mediterranean Journal of Pharmacy and Pharmaceutical Sciences 4 (2):69-74.
    Disintegration is the most important step for drug bioavailability because after, the disintegration process, the ingredients of solid dosage forms dissolve and become bioavailable. Generally, the tablets and capsules should be taken with a glass of water otherwise the manufacturer gives instructions to use the proper beverage. Several drugs are taken with different forms of beverages to ensure easy swallowing of the tablet, masking the bad taste of the drug and overcoming the drug aftertaste, these beverages can influence the (...)
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  48. Simple and Compound Drugs in Late Renaissance Medicine: The Pharmacology of Andrea Cesalpino (1593).Elisabeth Moreau - 2023 - In Fabrizio Baldassarri & Craig Martin, Andrea Cesalpino and Renaissance Aristotelianism. New York: Bloomsbury. pp. 209-223.
    From antiquity, Galenic physicians extensively discussed the active powers of simple and compound drugs. In their views, simple drugs, that is, single ingredients, acted according to their material qualities and the properties of their substance. As for compound drugs, their efficacy resulted from the mutual interaction of their ingredients and their modes of preparation. In the late Renaissance, Galenic physicians and naturalists, such as Leonhart Fuchs and Pietro Andrea Mattioli, attempted to explain these pharmacological properties or “faculties” (...)
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  49. Mandatory Minimums and the War on Drugs.Daniel Wodak - 2018 - In David Boonin, Palgrave Handbook of Philosophy and Public Policy. Cham: Palgrave Macmillan. pp. 51-62.
    Mandatory minimum sentencing provisions have been a feature of the U.S. justice system since 1790. But they have expanded considerably under the war on drugs, and their use has expanded considerably under the Trump Administration; some states are also poised to expand drug-related mandatory minimums further in efforts to fight the current opioid epidemic. In this paper I outline and evaluate three prominent arguments for and against the use of mandatory minimums in the war on drugs—they appeal, respectively, (...)
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  50. Might stimulant drugs support moral agency in ADHD children?Steven Edward Hyman - 2013 - Journal of Medical Ethics 39 (6):369-370.
    Stimulants have been shown to be safe and effective for reduction of the symptoms of attention deficit hyperactivity disorder. Despite much debate, however, there has been little empirical evidence as to whether stimulants affect authenticity and moral agency in children. Singh presents evidence that stimulants do not undercut children's' sense of self and increase their experience of agency. These findings are consistent with laboratory evidence that stimulant drugs in therapeutic doses improve cognitive control over thought and behavior.
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